Puig Carmen, Domenech Arnau, Garmendia Junkal, Langereis Jeroen D, Mayer Pascal, Calatayud Laura, Liñares Josefina, Ardanuy Carmen, Marti Sara
Microbiology Department, Hospital Universitari Bellvitge, IDIBELL-Universitat de Barcelona, Barcelona, Spain Research Network for Respiratory Diseases (CIBERES), ISCIII, Madrid, Spain.
Institute for Agrobiotechnology, CSIC-Public University of Navarra-Gobierno de Navarra, Mutilva, Spain Research Network for Respiratory Diseases (CIBERES), ISCIII, Madrid, Spain.
Appl Environ Microbiol. 2014 Nov;80(22):7088-95. doi: 10.1128/AEM.02544-14. Epub 2014 Sep 5.
Biofilm formation by nontypeable (NT) Haemophilus influenzae remains a controversial topic. Nevertheless, biofilm-like structures have been observed in the middle-ear mucosa of experimental chinchilla models of otitis media (OM). To date, there have been no studies of biofilm formation in large collections of clinical isolates. This study aimed to investigate the initial adhesion to a solid surface and biofilm formation by NT H. influenzae by comparing isolates from healthy carriers, those with noninvasive respiratory disease, and those with invasive respiratory disease. We used 352 isolates from patients with nonbacteremic community-acquired pneumonia (NB-CAP), chronic obstructive pulmonary disease (COPD), OM, and invasive disease and a group of healthy colonized children. We then determined the speed of initial adhesion to a solid surface by the BioFilm ring test and quantified biofilm formation by crystal violet staining. Isolates from different clinical sources displayed high levels of biofilm formation on a static solid support after growth for 24 h. We observed clear differences in initial attachment and biofilm formation depending on the pathology associated with NT H. influenzae isolation, with significantly increased biofilm formation for NT H. influenzae isolates collected from patients with invasive disease and OM compared with NT H. influenzae isolates from patients with NB-CAP or COPD and healthy colonized subjects. In all cases, biofilm structures were detached by proteinase K treatment, suggesting an important role for proteins in the initial adhesion and static biofilm formation measured by crystal violet staining.
不可分型(NT)流感嗜血杆菌形成生物膜仍然是一个有争议的话题。然而,在中耳炎(OM)实验性栗鼠模型的中耳黏膜中已观察到类似生物膜的结构。迄今为止,尚未有对大量临床分离株中生物膜形成的研究。本研究旨在通过比较来自健康携带者、患有非侵袭性呼吸道疾病者以及患有侵袭性呼吸道疾病者的分离株,来研究NT流感嗜血杆菌对固体表面的初始黏附及生物膜形成情况。我们使用了来自非菌血症社区获得性肺炎(NB-CAP)、慢性阻塞性肺疾病(COPD)、OM和侵袭性疾病患者以及一组健康定植儿童的352株分离株。然后,我们通过生物膜环试验确定对固体表面的初始黏附速度,并通过结晶紫染色对生物膜形成进行定量。在生长24小时后,来自不同临床来源的分离株在静态固体支持物上表现出高水平的生物膜形成。我们观察到,根据与NT流感嗜血杆菌分离相关的病理情况,初始黏附和生物膜形成存在明显差异,与来自NB-CAP或COPD患者以及健康定植受试者的NT流感嗜血杆菌分离株相比,从患有侵袭性疾病和OM的患者中收集的NT流感嗜血杆菌分离株的生物膜形成显著增加。在所有情况下,生物膜结构经蛋白酶K处理后会脱落,这表明蛋白质在通过结晶紫染色测定的初始黏附和静态生物膜形成中起重要作用。